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(2S,6S)-ethyl 3,6-dihydro-6-methoxy-2H-pyran-2-carboxylate | 920537-36-6

中文名称
——
中文别名
——
英文名称
(2S,6S)-ethyl 3,6-dihydro-6-methoxy-2H-pyran-2-carboxylate
英文别名
ethyl (2S,6S)-6-methoxy-3,6-dihydro-2H-pyran-2-carboxylate
(2S,6S)-ethyl 3,6-dihydro-6-methoxy-2H-pyran-2-carboxylate化学式
CAS
920537-36-6
化学式
C9H14O4
mdl
——
分子量
186.208
InChiKey
ZOTGPTQNWLHTNN-YUMQZZPRSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    1.1
  • 重原子数:
    13
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    44.8
  • 氢给体数:
    0
  • 氢受体数:
    4

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    (2S,6S)-ethyl 3,6-dihydro-6-methoxy-2H-pyran-2-carboxylate 在 lithium aluminium tetrahydride 作用下, 以 乙醚 为溶剂, 反应 3.0h, 以55%的产率得到(2S,6S)-6-hydroxymethyl-2-methoxy-5,6-dihydro-2H-pyran
    参考文献:
    名称:
    Chiral Phosphoric Acid-Governed Anti-Diastereoselective and Enantioselective Hetero-Diels−Alder Reaction of Glyoxylate
    摘要:
    A highly enantioselective anti-diastereoselective hetero-Diets-Alder reaction between a glyoxylate and siloxy- or methoxydienes using a chiral phosphoric acid catalyst that possesses less bulky phenyl groups at the 3 and 3' positions of binaphthyl has been developed. The diastereoselectivities presented are disparate to those previously reported for hetero-Diets-Alder reactions catalyzed by a chiral Lewis acid.
    DOI:
    10.1021/ja904749x
  • 作为产物:
    描述:
    乙醛酸乙酯1-甲氧基-1,3-丁二烯(Ra)-4-hydroxy-2,6-diphenyldinaphtho[1,3,2]dioxaphosphepine 4-oxide 作用下, 以 甲苯 为溶剂, 反应 24.0h, 生成 ethyl 2-methoxy-5,6-dihydro-2H-pyran-6-carboxylate 、 (2S,6S)-ethyl 3,6-dihydro-6-methoxy-2H-pyran-2-carboxylate
    参考文献:
    名称:
    Chiral Phosphoric Acid-Governed Anti-Diastereoselective and Enantioselective Hetero-Diels−Alder Reaction of Glyoxylate
    摘要:
    A highly enantioselective anti-diastereoselective hetero-Diets-Alder reaction between a glyoxylate and siloxy- or methoxydienes using a chiral phosphoric acid catalyst that possesses less bulky phenyl groups at the 3 and 3' positions of binaphthyl has been developed. The diastereoselectivities presented are disparate to those previously reported for hetero-Diets-Alder reactions catalyzed by a chiral Lewis acid.
    DOI:
    10.1021/ja904749x
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文献信息

  • Chiral Phosphoric Acid-Governed Anti-Diastereoselective and Enantioselective Hetero-Diels−Alder Reaction of Glyoxylate
    作者:Norie Momiyama、Hideaki Tabuse、Masahiro Terada
    DOI:10.1021/ja904749x
    日期:2009.9.16
    A highly enantioselective anti-diastereoselective hetero-Diets-Alder reaction between a glyoxylate and siloxy- or methoxydienes using a chiral phosphoric acid catalyst that possesses less bulky phenyl groups at the 3 and 3' positions of binaphthyl has been developed. The diastereoselectivities presented are disparate to those previously reported for hetero-Diets-Alder reactions catalyzed by a chiral Lewis acid.
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